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Nucleic Acids Research 2005 33(1):347-355; doi:10.1093/nar/gki183
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Published online 13 January 2005

© 2005, the authors Nucleic Acids Research, Vol. 33 No. 1 © Oxford University Press 2005; all rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use permissions, please contact journals.permissions{at}oupjournals.org.


Article

RDE-2 interacts with MUT-7 to mediate RNA interference in Caenorhabditis elegans

Bastiaan B. J. Tops, Hiroaki Tabara1, Titia Sijen, Femke Simmer, Craig C. Mello1, Ronald H. A. Plasterk* and René F. Ketting

Hubrecht Laboratory, Centre for Biomedical Genetics Uppsalalaan 8, 3584 CT Utrecht, The Netherlands 1 Department of Cell Biology, Program in Molecular Medicine, University of Massachusetts Cancer Centre Worcester, MA 01605, USA

*To whom correspondence should be addressed. Tel: +31 30 212 1963; Fax: +31 30 251 6554; Email: plasterk{at}niob.knaw.nl

Received December 7, 2004. Revised December 21, 2004. Accepted December 21, 2004.

In Caenorhabditis elegans, the activity of transposable elements is repressed in the germline. One of the mechanisms involved in this repression is RNA interference (RNAi), a process in which dsRNA targets cleavage of mRNAs in a sequence-specific manner. The first gene found to be involved in RNAi and transposon silencing in C.elegans is mut-7, a gene encoding a putative exoribonuclease. Here, we show that the MUT-7 protein resides in complexes of ~250 kDa in the nucleus and in the cytosol. In addition, we find that upon triggering of RNAi the cytosolic MUT-7 complex increases in size. This increase is independent of the presence of target RNA, but does depend on the presence of RDE-1 and RDE-4, two proteins involved in small interfering RNA (siRNA) production. Finally, using a yeast two-hybrid screen, we identified RDE-2/MUT-8 as one of the other components of this complex. This protein is encoded by the rde-2/mut-8 locus, previously implicated in RNAi and transposon silencing. Using genetic complementation analysis, we show that the interaction between these two proteins is required for efficient RNAi in vivo. Together these data support a role for the MUT-7/RDE-2 complex downstream of siRNA formation, but upstream of siRNA mediated target RNA recognition, possibly indicating a role in the siRNA amplification step.


Correspondence may also be addressed to René F. Ketting. Tel: +31 30 212 1964; Fax: +31 30 251 6554; Email: ketting{at}niob.knaw.nl

Present address: Hiroaki Tabara, Kyoto University, Graduate School of Medicine, HMRO, Yoshida-Konoe, Sakyo, Kyoto 606-8501, Japan


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